BDKRB2 Gene

Bradykinin Receptor B2 (BDKRB2) is a gene involved in bradykinin signaling that has been studied in relation to immune function, metabolism, and chronic illness. Variants in BDKRB2 may influence how the body responds to infection, inflammation, and long-term recovery.

This page is for educational and informational purposes only. Not a diagnostic tool. Always consult a qualified healthcare provider.

What is the BDKRB2 gene?

BDKRB2 encodes bradykinin receptor b2, a protein involved in bradykinin signaling. It belongs to the Cardiovascular category and is part of the Coagulation & Vascular biological cluster. BDKRB2 is the constitutively expressed high-affinity receptor for bradykinin mediating vasodilation, vascular permeability, pain sensitization, and inflammation. ACE2 and ACE are key regulators of bradykinin degradation.

Biological role and pathway

BDKRB2 is involved in the bradykinin signaling pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Coagulation & Vascular cluster work together to maintain balanced function across interconnected biological systems.

Variants in genes within this pathway may influence an individual's predisposition to altered function in these systems — particularly under conditions of physiological stress such as viral infection or prolonged illness.

BDKRB2 and Long COVID / ME-CFS research

A bradykinin storm (kinin excess from impaired ACE/ACE2 degradation) is proposed in COVID-19 pathogenesis. BDKRB2 variants affecting bradykinin signaling intensity may influence vascular inflammation, edema, hypotension, and POTS-like symptoms in Long COVID.

This information is based on published research and does not constitute medical advice. See references below.

Known genetic variants

The following variants (SNPs) in the BDKRB2 gene have been studied in relation to cardiovascular and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.

Conditions studied in relation to BDKRB2

Research into BDKRB2 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that BDKRB2 causes or treats any condition.

Genetic insights from DNA data

Consumer DNA files from 23andMe, AncestryDNA, and MyHeritage contain raw SNP data. When you upload your file to ChronicDNA, the analysis engine checks your genotype against a curated panel of 80+ genes selected for their relevance to Long COVID, ME/CFS, and connected biological pathways - some of which may include BDKRB2 and related genes in the coagulation & vascular pathway.

The report is educational - it explains which variants you carry, what the research says about them, and how they fit into the biological pathways most relevant to chronic illness. Results are presented in plain English with appropriate scientific context, no medical jargon, no scare tactics. All results should be discussed with a qualified healthcare provider.

Related genes in the Coagulation & Vascular pathway

BDKRB2 does not act in isolation. The following genes are functionally related and may be analysed together for a more complete picture of your genetic predispositions.

Frequently asked questions

What is the BDKRB2 gene and what does it do?

BDKRB2 (Bradykinin Receptor B2) is involved in bradykinin signaling. BDKRB2 is the constitutively expressed high-affinity receptor for bradykinin mediating vasodilation, vascular permeability, pain sensitization, and inflammation. ACE2 and ACE are key regulators of bradykinin degradation.

How may BDKRB2 gene variants relate to Long COVID or ME/CFS?

A bradykinin storm (kinin excess from impaired ACE/ACE2 degradation) is proposed in COVID-19 pathogenesis. BDKRB2 variants affecting bradykinin signaling intensity may influence vascular inflammation, edema, hypotension, and POTS-like symptoms in Long COVID.

Can a DNA test reveal information about my BDKRB2 gene?

Consumer DNA data from 23andMe, AncestryDNA, and MyHeritage includes SNP variants for many genes. ChronicDNA analyses your raw DNA file and reports on variants that have been studied in relation to chronic illness, immune function, and metabolism. This is not a diagnostic service — results are informational and educational only.

Explore your BDKRB2 genetic insights

Upload your DNA data from 23andMe, AncestryDNA, or MyHeritage and receive a personalised report covering >80 genes relevant to Long COVID and ME/CFS.

Get Your Personalised DNA Report

Informational and educational only · Not a diagnostic tool · GDPR compliant

References

The following publications were used in compiling the research context for BDKRB2. This is not an exhaustive literature review.

  • [1]PMID: 32826326
  • [2]Science
  • [3]Hypertension